| 8649980 | CV126554 | single nucleotide variant | NM_001115.2(ADCY8):c.961-9428T>A | Lung cancer [RCV000107041] | uncertain significance | 8 | 130999970 | 130999970 | Human | | name |
| 8649981 | CV126555 | single nucleotide variant | NM_001115.2(ADCY8):c.960+23203T>C | Lung cancer [RCV000107042] | uncertain significance | 8 | 131016171 | 131016171 | Human | | name |
| 155991606 | CV2255692 | single nucleotide variant | NM_001115.3(ADCY8):c.7C>T (p.Leu3Phe) | not specified [RCV004120092] | uncertain significance | 8 | 131040327 | 131040327 | Human | | name |
| 598232624 | CV3948419 | single nucleotide variant | NM_001115.3(ADCY8):c.20G>T (p.Arg7Leu) | not specified [RCV005319786] | uncertain significance | 8 | 131040314 | 131040314 | Human | | name |
| 401752959 | CV2703603 | single nucleotide variant | NM_001115.3(ADCY8):c.79G>C (p.Gly27Arg) | not specified [RCV004317769] | uncertain significance | 8 | 131040255 | 131040255 | Human | | name |
| 401889911 | CV2755397 | single nucleotide variant | NM_001115.3(ADCY8):c.88G>T (p.Ala30Ser) | not specified [RCV004337559] | uncertain significance | 8 | 131040246 | 131040246 | Human | | name |
| 401893077 | CV2758453 | single nucleotide variant | NM_001115.3(ADCY8):c.73G>A (p.Gly25Ser) | not specified [RCV004335105] | uncertain significance | 8 | 131040261 | 131040261 | Human | | name |
| 407464575 | CV3429803 | single nucleotide variant | NM_001115.3(ADCY8):c.87C>G (p.Ser29Arg) | not specified [RCV004613490] | uncertain significance | 8 | 131040247 | 131040247 | Human | | name |
| 597773096 | CV3660772 | single nucleotide variant | NM_001115.3(ADCY8):c.74G>A (p.Gly25Asp) | not specified [RCV004897487] | uncertain significance | 8 | 131040260 | 131040260 | Human | | name |
| 598232576 | CV3948409 | single nucleotide variant | NM_001115.3(ADCY8):c.52A>G (p.Ile18Val) | not specified [RCV005319776] | uncertain significance | 8 | 131040282 | 131040282 | Human | | name |
| 15146055 | CV711287 | single nucleotide variant | NM_001115.3(ADCY8):c.945C>T (p.Val315=) | not provided [RCV000967102] | benign | 8 | 131039389 | 131039389 | Human | | name |
| 8632849 | CV88064 | single nucleotide variant | NM_001115.2(ADCY8):c.771C>T (p.Ile257=) | Malignant melanoma [RCV000068156] | not provided | 8 | 131039563 | 131039563 | Human | | name |
| 155963666 | CV2197983 | single nucleotide variant | NM_001115.3(ADCY8):c.215C>A (p.Ala72Glu) | not specified [RCV004077193] | uncertain significance | 8 | 131040119 | 131040119 | Human | | name |
| 155931135 | CV2297238 | single nucleotide variant | NM_001115.3(ADCY8):c.163C>T (p.Arg55Trp) | not specified [RCV004151118] | uncertain significance | 8 | 131040171 | 131040171 | Human | | name |
| 156210411 | CV2314260 | single nucleotide variant | NM_001115.3(ADCY8):c.194C>G (p.Ser65Trp) | not specified [RCV004166621] | uncertain significance | 8 | 131040140 | 131040140 | Human | | name |
| 156154308 | CV2369494 | single nucleotide variant | NM_001115.3(ADCY8):c.296G>A (p.Arg99Gln) | not specified [RCV004210431] | uncertain significance | 8 | 131040038 | 131040038 | Human | | name |
| 155960417 | CV2390687 | single nucleotide variant | NM_001115.3(ADCY8):c.275A>T (p.Tyr92Phe) | not specified [RCV004239201] | uncertain significance | 8 | 131040059 | 131040059 | Human | | name |
| 329370011 | CV2461310 | single nucleotide variant | NM_001115.3(ADCY8):c.130C>A (p.His44Asn) | not specified [RCV004267480] | uncertain significance | 8 | 131040204 | 131040204 | Human | | name |
| 401758162 | CV2704209 | single nucleotide variant | NM_001115.3(ADCY8):c.256G>T (p.Asp86Tyr) | not specified [RCV004311213] | uncertain significance | 8 | 131040078 | 131040078 | Human | | name |
| 401858918 | CV2774976 | single nucleotide variant | NM_001115.3(ADCY8):c.260C>T (p.Ser87Leu) | not specified [RCV004346374] | uncertain significance | 8 | 131040074 | 131040074 | Human | | name |
| 405692945 | CV3243742 | single nucleotide variant | NM_001115.3(ADCY8):c.211C>G (p.Pro71Ala) | not specified [RCV004373633] | uncertain significance | 8 | 131040123 | 131040123 | Human | | name |
| 407464845 | CV3429872 | single nucleotide variant | NM_001115.3(ADCY8):c.205T>A (p.Ser69Thr) | not specified [RCV004613559] | uncertain significance | 8 | 131040129 | 131040129 | Human | | name |
| 597773118 | CV3660787 | single nucleotide variant | NM_001115.3(ADCY8):c.157G>C (p.Gly53Arg) | not specified [RCV004897491] | uncertain significance | 8 | 131040177 | 131040177 | Human | | name |
| 598242873 | CV3944517 | single nucleotide variant | NM_001115.3(ADCY8):c.194C>T (p.Ser65Leu) | not specified [RCV005321817] | uncertain significance | 8 | 131040140 | 131040140 | Human | | name |
| 598232493 | CV3948389 | single nucleotide variant | NM_001115.3(ADCY8):c.278C>T (p.Ser93Leu) | not specified [RCV005319756] | uncertain significance | 8 | 131040056 | 131040056 | Human | | name |
| 598242737 | CV3948433 | single nucleotide variant | NM_001115.3(ADCY8):c.124G>C (p.Val42Leu) | not specified [RCV005321792] | uncertain significance | 8 | 131040210 | 131040210 | Human | | name |
| 15146047 | CV711282 | single nucleotide variant | NM_001115.3(ADCY8):c.2976G>A (p.Ala992=) | not provided [RCV000967101] | benign | 8 | 130800510 | 130800510 | Human | | name |
| 15132179 | CV736427 | single nucleotide variant | NM_001115.3(ADCY8):c.1551C>T (p.Cys517=) | not provided [RCV000897910] | likely benign | 8 | 130909797 | 130909797 | Human | | name |
| 15161952 | CV750905 | single nucleotide variant | NM_001115.3(ADCY8):c.2949G>A (p.Val983=) | not provided [RCV000925791] | likely benign | 8 | 130800537 | 130800537 | Human | | name |
| 8626534 | CV81678 | single nucleotide variant | NM_001115.2(ADCY8):c.2382G>A (p.Leu794=) | Malignant melanoma [RCV000061756] | not provided | 8 | 130849632 | 130849632 | Human | | name |
| 8632843 | CV88058 | single nucleotide variant | NM_001115.2(ADCY8):c.2391C>T (p.Phe797=) | Malignant melanoma [RCV000068150] | not provided | 8 | 130849623 | 130849623 | Human | | name |
| 156192497 | CV2202398 | single nucleotide variant | NM_001115.3(ADCY8):c.877A>T (p.Ile293Phe) | not specified [RCV004080712] | uncertain significance | 8 | 131039457 | 131039457 | Human | | name |
| 156093768 | CV2213198 | single nucleotide variant | NM_001115.3(ADCY8):c.559G>T (p.Val187Leu) | not specified [RCV004085425] | uncertain significance | 8 | 131039775 | 131039775 | Human | | name |
| 155900852 | CV2298043 | single nucleotide variant | NM_001115.3(ADCY8):c.346G>T (p.Gly116Cys) | not specified [RCV004157938] | uncertain significance | 8 | 131039988 | 131039988 | Human | | name |
| 156253632 | CV2366238 | single nucleotide variant | NM_001115.3(ADCY8):c.329C>A (p.Pro110Gln) | not specified [RCV004210254] | uncertain significance | 8 | 131040005 | 131040005 | Human | | name |
| 156174085 | CV2377145 | single nucleotide variant | NM_001115.3(ADCY8):c.781G>A (p.Gly261Ser) | not specified [RCV004231822] | uncertain significance | 8 | 131039553 | 131039553 | Human | | name |
| 401740942 | CV2702708 | single nucleotide variant | NM_001115.3(ADCY8):c.691G>C (p.Val231Leu) | not specified [RCV004318961] | uncertain significance | 8 | 131039643 | 131039643 | Human | | name |
| 401733546 | CV2713127 | single nucleotide variant | NM_001115.3(ADCY8):c.436G>T (p.Gly146Cys) | not specified [RCV004316677] | uncertain significance | 8 | 131039898 | 131039898 | Human | | name |
| 401891312 | CV2768991 | single nucleotide variant | NM_001115.3(ADCY8):c.879C>G (p.Ile293Met) | not specified [RCV004348866] | uncertain significance | 8 | 131039455 | 131039455 | Human | | name |
| 401893888 | CV2774178 | single nucleotide variant | NM_001115.3(ADCY8):c.869C>T (p.Thr290Ile) | not specified [RCV004345767] | uncertain significance | 8 | 131039465 | 131039465 | Human | | name |
| 405693187 | CV3243788 | single nucleotide variant | NM_001115.3(ADCY8):c.344G>A (p.Ser115Asn) | not specified [RCV004373679] | uncertain significance | 8 | 131039990 | 131039990 | Human | | name |
| 405693300 | CV3243808 | single nucleotide variant | NM_001115.3(ADCY8):c.515G>T (p.Arg172Leu) | not specified [RCV004373699] | uncertain significance | 8 | 131039819 | 131039819 | Human | | name |
| 407464699 | CV3429833 | single nucleotide variant | NM_001115.3(ADCY8):c.986T>C (p.Met329Thr) | not specified [RCV004613520] | uncertain significance | 8 | 130990517 | 130990517 | Human | | name |
| 597773036 | CV3660759 | single nucleotide variant | NM_001115.3(ADCY8):c.346G>A (p.Gly116Ser) | not specified [RCV004897474] | uncertain significance | 8 | 131039988 | 131039988 | Human | | name |
| 597773108 | CV3660777 | single nucleotide variant | NM_001115.3(ADCY8):c.403G>T (p.Ala135Ser) | not specified [RCV004897489] | uncertain significance | 8 | 131039931 | 131039931 | Human | | name |
| 597773113 | CV3660782 | single nucleotide variant | NM_001115.3(ADCY8):c.627C>A (p.Asp209Glu) | not specified [RCV004897490] | uncertain significance | 8 | 131039707 | 131039707 | Human | | name |
| 597773159 | CV3660841 | single nucleotide variant | NM_001115.3(ADCY8):c.869C>G (p.Thr290Ser) | not specified [RCV004897499] | uncertain significance | 8 | 131039465 | 131039465 | Human | | name |
| 597773192 | CV3660848 | single nucleotide variant | NM_001115.3(ADCY8):c.611C>G (p.Ala204Gly) | not specified [RCV004897505] | uncertain significance | 8 | 131039723 | 131039723 | Human | | name |
| 597773286 | CV3660867 | single nucleotide variant | NM_001115.3(ADCY8):c.931C>T (p.Pro311Ser) | not specified [RCV004897523] | uncertain significance | 8 | 131039403 | 131039403 | Human | | name |
| 598243057 | CV3944550 | single nucleotide variant | NM_001115.3(ADCY8):c.498G>C (p.Leu166Phe) | not specified [RCV005321846] | uncertain significance | 8 | 131039836 | 131039836 | Human | | name |
| 598243114 | CV3944560 | single nucleotide variant | NM_001115.3(ADCY8):c.691G>A (p.Val231Met) | not specified [RCV005321856] | uncertain significance | 8 | 131039643 | 131039643 | Human | | name |
| 598232654 | CV3948426 | single nucleotide variant | NM_001115.3(ADCY8):c.472C>A (p.Arg158Ser) | not specified [RCV005319793] | uncertain significance | 8 | 131039862 | 131039862 | Human | | name |
| 15179836 | CV722846 | single nucleotide variant | NM_001115.3(ADCY8):c.3612T>C (p.Asn1204=) | not provided [RCV000885382] | benign | 8 | 130780534 | 130780534 | Human | | name |
| 15179841 | CV722847 | single nucleotide variant | NM_001115.3(ADCY8):c.3582G>A (p.Ala1194=) | not provided [RCV000885383] | benign | 8 | 130780564 | 130780564 | Human | | name |
| 8626533 | CV81677 | single nucleotide variant | NM_001115.2(ADCY8):c.3537C>T (p.Phe1179=) | Malignant melanoma [RCV000061755] | not provided | 8 | 130780609 | 130780609 | Human | | name |
| 8632848 | CV88063 | single nucleotide variant | NM_001115.2(ADCY8):c.993G>A (p.Met331Ile) | Malignant melanoma [RCV000068155] | not provided | 8 | 130990510 | 130990510 | Human | | name |
| 156243275 | CV2210896 | single nucleotide variant | NM_001115.3(ADCY8):c.1343G>A (p.Arg448Gln) | not specified [RCV004085974] | uncertain significance | 8 | 130943361 | 130943361 | Human | | name |
| 155951614 | CV2264123 | single nucleotide variant | NM_001115.3(ADCY8):c.2435C>T (p.Ser812Leu) | not specified [RCV004136283] | uncertain significance | 8 | 130847491 | 130847491 | Human | | name |
| 156100382 | CV2294706 | single nucleotide variant | NM_001115.3(ADCY8):c.1177G>A (p.Val393Met) | not specified [RCV004161950] | uncertain significance | 8 | 130951932 | 130951932 | Human | | name |
| 156388774 | CV2376064 | single nucleotide variant | NM_001115.3(ADCY8):c.1664C>T (p.Thr555Met) | not specified [RCV004220302] | uncertain significance | 8 | 130904019 | 130904019 | Human | | name |
| 156190601 | CV2385012 | single nucleotide variant | NM_001115.3(ADCY8):c.2082G>A (p.Met694Ile) | not specified [RCV004228282] | uncertain significance | 8 | 130884591 | 130884591 | Human | | name |
| 156006743 | CV2394226 | single nucleotide variant | NM_001115.3(ADCY8):c.2881C>T (p.Arg961Cys) | not specified [RCV004238464] | uncertain significance | 8 | 130814101 | 130814101 | Human | | name |
| 329357029 | CV2460661 | single nucleotide variant | NM_001115.3(ADCY8):c.1132C>T (p.Leu378Phe) | not specified [RCV004270708] | uncertain significance | 8 | 130951977 | 130951977 | Human | | name |
| 401772570 | CV2719682 | single nucleotide variant | NM_001115.3(ADCY8):c.2164G>A (p.Val722Ile) | not specified [RCV004329126] | uncertain significance | 8 | 130867892 | 130867892 | Human | | name |
| 401718151 | CV2721516 | single nucleotide variant | NM_001115.3(ADCY8):c.1636C>T (p.Pro546Ser) | not specified [RCV004316032] | uncertain significance | 8 | 130909712 | 130909712 | Human | | name |
| 401896465 | CV2781413 | single nucleotide variant | NM_001115.3(ADCY8):c.1682G>A (p.Gly561Asp) | not specified [RCV004352416] | uncertain significance | 8 | 130904001 | 130904001 | Human | | name |
| 405692801 | CV3243713 | single nucleotide variant | NM_001115.3(ADCY8):c.1115G>A (p.Arg372Gln) | not specified [RCV004373604] | uncertain significance | 8 | 130951994 | 130951994 | Human | | name |
| 405692819 | CV3243716 | single nucleotide variant | NM_001115.3(ADCY8):c.1139G>A (p.Arg380Gln) | not specified [RCV004373607] | uncertain significance | 8 | 130951970 | 130951970 | Human | | name |
| 405692878 | CV3243729 | single nucleotide variant | NM_001115.3(ADCY8):c.1681G>A (p.Gly561Ser) | not specified [RCV004373620] | uncertain significance | 8 | 130904002 | 130904002 | Human | | name |
| 405692912 | CV3243736 | single nucleotide variant | NM_001115.3(ADCY8):c.2078T>C (p.Leu693Pro) | not specified [RCV004373627] | uncertain significance | 8 | 130884595 | 130884595 | Human | | name |
| 405692792 | CV3247223 | single nucleotide variant | NM_001115.3(ADCY8):c.1024T>C (p.Ser342Pro) | not specified [RCV004373602] | uncertain significance | 8 | 130990479 | 130990479 | Human | | name |
| 407464619 | CV3429813 | single nucleotide variant | NM_001115.3(ADCY8):c.1189C>T (p.His397Tyr) | not specified [RCV004613500] | uncertain significance | 8 | 130951920 | 130951920 | Human | | name |
| 407464663 | CV3429824 | single nucleotide variant | NM_001115.3(ADCY8):c.1172C>T (p.Thr391Ile) | not specified [RCV004613511] | uncertain significance | 8 | 130951937 | 130951937 | Human | | name |
| 407464770 | CV3429854 | single nucleotide variant | NM_001115.3(ADCY8):c.2384T>C (p.Ile795Thr) | not specified [RCV004613541] | uncertain significance | 8 | 130849630 | 130849630 | Human | | name |
| 597773102 | CV3660773 | single nucleotide variant | NM_001115.3(ADCY8):c.2026G>A (p.Asp676Asn) | not specified [RCV004897488] | uncertain significance | 8 | 130884647 | 130884647 | Human | | name |
| 597773123 | CV3660797 | single nucleotide variant | NM_001115.3(ADCY8):c.2906A>C (p.Asp969Ala) | not specified [RCV004897492] | uncertain significance | 8 | 130814076 | 130814076 | Human | | name |
| 597773128 | CV3660807 | single nucleotide variant | NM_001115.3(ADCY8):c.1343G>C (p.Arg448Pro) | not specified [RCV004897493] | uncertain significance | 8 | 130943361 | 130943361 | Human | | name |
| 597773134 | CV3660808 | single nucleotide variant | NM_001115.3(ADCY8):c.1306G>C (p.Val436Leu) | not specified [RCV004897494] | uncertain significance | 8 | 130943398 | 130943398 | Human | | name |
| 597773139 | CV3660811 | single nucleotide variant | NM_001115.3(ADCY8):c.1894A>G (p.Ile632Val) | not specified [RCV004897495] | uncertain significance | 8 | 130903789 | 130903789 | Human | | name |
| 597773144 | CV3660816 | single nucleotide variant | NM_001115.3(ADCY8):c.1856C>T (p.Thr619Ile) | not specified [RCV004897496] | uncertain significance | 8 | 130903827 | 130903827 | Human | | name |
| 597773149 | CV3660822 | single nucleotide variant | NM_001115.3(ADCY8):c.2533G>A (p.Val845Met) | not specified [RCV004897497] | uncertain significance | 8 | 130836419 | 130836419 | Human | | name |
| 597773154 | CV3660832 | single nucleotide variant | NM_001115.3(ADCY8):c.2516C>T (p.Thr839Met) | not specified [RCV004897498] | uncertain significance | 8 | 130836436 | 130836436 | Human | | name |
| 597773235 | CV3660856 | single nucleotide variant | NM_001115.3(ADCY8):c.1438C>T (p.His480Tyr) | not specified [RCV004897513] | uncertain significance | 8 | 130937116 | 130937116 | Human | | name |
| 598242764 | CV3944498 | single nucleotide variant | NM_001115.3(ADCY8):c.2378T>C (p.Ile793Thr) | not specified [RCV005321798] | uncertain significance | 8 | 130849636 | 130849636 | Human | | name |
| 598242998 | CV3944539 | single nucleotide variant | NM_001115.3(ADCY8):c.2021C>T (p.Thr674Ile) | not specified [RCV005321837] | uncertain significance | 8 | 130884652 | 130884652 | Human | | name |
| 598243176 | CV3944570 | single nucleotide variant | NM_001115.3(ADCY8):c.2091C>G (p.Asp697Glu) | not specified [RCV005321866] | uncertain significance | 8 | 130884582 | 130884582 | Human | | name |
| 598232596 | CV3948413 | single nucleotide variant | NM_001115.3(ADCY8):c.1370G>A (p.Arg457His) | not specified [RCV005319780] | uncertain significance | 8 | 130937184 | 130937184 | Human | | name |
| 8626535 | CV81679 | single nucleotide variant | NM_001115.2(ADCY8):c.2041G>A (p.Asp681Asn) | Malignant melanoma [RCV000061757] | not provided | 8 | 130884632 | 130884632 | Human | | name |
| 8632842 | CV88057 | single nucleotide variant | NM_001115.2(ADCY8):c.2595G>A (p.Met865Ile) | Malignant melanoma [RCV000068149] | not provided | 8 | 130836357 | 130836357 | Human | | name |
| 8632844 | CV88059 | single nucleotide variant | NM_001115.2(ADCY8):c.2333T>A (p.Ile778Asn) | Malignant melanoma [RCV000068151] | not provided | 8 | 130849681 | 130849681 | Human | | name |
| 8632845 | CV88060 | single nucleotide variant | NM_001115.2(ADCY8):c.1996G>A (p.Glu666Lys) | Malignant melanoma [RCV000068152] | not provided | 8 | 130884677 | 130884677 | Human | | name |
| 8632846 | CV88061 | single nucleotide variant | NM_001115.2(ADCY8):c.1300G>A (p.Glu434Lys) | Malignant melanoma [RCV000068153] | not provided | 8 | 130943404 | 130943404 | Human | | name |
| 8632847 | CV88062 | single nucleotide variant | NM_001115.2(ADCY8):c.1158G>A (p.Met386Ile) | Malignant melanoma [RCV000068154] | not provided | 8 | 130951951 | 130951951 | Human | | name |
| 156400459 | CV2199196 | single nucleotide variant | NM_001115.3(ADCY8):c.3205G>A (p.Ala1069Thr) | not specified [RCV004080583] | uncertain significance | 8 | 130783754 | 130783754 | Human | | name |
| 155987962 | CV2234160 | single nucleotide variant | NM_001115.3(ADCY8):c.3382G>A (p.Gly1128Ser) | not specified [RCV004106249] | uncertain significance | 8 | 130780764 | 130780764 | Human | | name |
| 155918649 | CV2236876 | single nucleotide variant | NM_001115.3(ADCY8):c.3449G>A (p.Arg1150Gln) | not specified [RCV004112632] | uncertain significance | 8 | 130780697 | 130780697 | Human | | name |
| 156088514 | CV2259055 | single nucleotide variant | NM_001115.3(ADCY8):c.3581C>T (p.Ala1194Val) | not specified [RCV004120319] | uncertain significance | 8 | 130780565 | 130780565 | Human | | name |
| 156072281 | CV2267463 | single nucleotide variant | NM_001115.3(ADCY8):c.3158G>A (p.Cys1053Tyr) | not specified [RCV004135893] | uncertain significance | 8 | 130783801 | 130783801 | Human | | name |
| 156255425 | CV2325747 | single nucleotide variant | NM_001115.3(ADCY8):c.3376G>T (p.Val1126Phe) | not specified [RCV004173641] | uncertain significance | 8 | 130780770 | 130780770 | Human | | name |
| 156278679 | CV2330940 | single nucleotide variant | NM_001115.3(ADCY8):c.3533C>A (p.Pro1178Gln) | not specified [RCV004185986] | uncertain significance | 8 | 130780613 | 130780613 | Human | | name |
| 156038083 | CV2374126 | single nucleotide variant | NM_001115.3(ADCY8):c.3682C>T (p.Arg1228Trp) | not specified [RCV004229284] | uncertain significance | 8 | 130780464 | 130780464 | Human | | name |
| 156247732 | CV2396933 | single nucleotide variant | NM_001115.3(ADCY8):c.3532C>G (p.Pro1178Ala) | not specified [RCV004234048] | uncertain significance | 8 | 130780614 | 130780614 | Human | | name |
| 401753054 | CV2674764 | single nucleotide variant | NM_001115.3(ADCY8):c.3456G>C (p.Glu1152Asp) | not specified [RCV004294044] | uncertain significance | 8 | 130780690 | 130780690 | Human | | name |
| 401733794 | CV2687835 | single nucleotide variant | NM_001115.3(ADCY8):c.3160G>A (p.Glu1054Lys) | not specified [RCV004303144] | uncertain significance | 8 | 130783799 | 130783799 | Human | | name |
| 401728526 | CV2729624 | single nucleotide variant | NM_001115.3(ADCY8):c.3680G>A (p.Arg1227Gln) | not specified [RCV004331886] | uncertain significance | 8 | 130780466 | 130780466 | Human | | name |
| 405693113 | CV3243774 | single nucleotide variant | NM_001115.3(ADCY8):c.3181T>C (p.Cys1061Arg) | not specified [RCV004373665] | uncertain significance | 8 | 130783778 | 130783778 | Human | | name |
| 405693236 | CV3243797 | single nucleotide variant | NM_001115.3(ADCY8):c.3472A>T (p.Ile1158Phe) | not specified [RCV004373688] | uncertain significance | 8 | 130780674 | 130780674 | Human | | name |
| 405693258 | CV3243801 | single nucleotide variant | NM_001115.3(ADCY8):c.3580G>A (p.Ala1194Thr) | not specified [RCV004373692] | uncertain significance | 8 | 130780566 | 130780566 | Human | | name |
| 407464734 | CV3429843 | single nucleotide variant | NM_001115.3(ADCY8):c.3429G>C (p.Gln1143His) | not specified [RCV004613530] | uncertain significance | 8 | 130780717 | 130780717 | Human | | name |
| 407464809 | CV3429863 | single nucleotide variant | NM_001115.3(ADCY8):c.3064C>T (p.Leu1022Phe) | not specified [RCV004613550] | uncertain significance | 8 | 130785472 | 130785472 | Human | | name |
| 597773030 | CV3660753 | single nucleotide variant | NM_001115.3(ADCY8):c.3164A>T (p.Asp1055Val) | not specified [RCV004897473] | uncertain significance | 8 | 130783795 | 130783795 | Human | | name |
| 598242813 | CV3944507 | single nucleotide variant | NM_001115.3(ADCY8):c.3500C>G (p.Thr1167Arg) | not specified [RCV005321807] | uncertain significance | 8 | 130780646 | 130780646 | Human | | name |
| 598242944 | CV3944529 | single nucleotide variant | NM_001115.3(ADCY8):c.3055G>A (p.Asp1019Asn) | not specified [RCV005321828] | uncertain significance | 8 | 130800431 | 130800431 | Human | | name |
| 598232538 | CV3948400 | single nucleotide variant | NM_001115.3(ADCY8):c.3410A>G (p.Tyr1137Cys) | not specified [RCV005319767] | uncertain significance | 8 | 130780736 | 130780736 | Human | | name |
| 8632841 | CV88056 | single nucleotide variant | NM_001115.2(ADCY8):c.3488G>A (p.Gly1163Glu) | Malignant melanoma [RCV000068148] | not provided | 8 | 130780658 | 130780658 | Human | | name |
